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生物鹼

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首个被分离出的生物碱,吗啡,于1804年由罂粟中提取。

生物鹼(英語:alkaloid)是一種天然存在的含氮鹼性化合物。一些人工合成但結構类似的化合物有時也被稱作生物鹼。除了,生物鹼也可以含有等元素。 生物鹼与其它含氮碱性化合物之间的分界并不明确,但氨基酸核苷酸类物质通常不被称作生物碱。

生物鹼在人或動物体内产生藥理反應。雖然大部份的生物鹼對人體有毒,但有些也能入药,起鎮痛或麻醉的作用,以嗎啡可待因尤为重要。生物鹼大都是氨基酸衍生物,嚐起來有苦澀味,是植物(如馬鈴薯蕃茄罂粟)、動物(如貝类)、细菌真菌等多种生命体的次生代谢物。通过对生物体的粗提取物进行酸碱萃取纯化,可以获得大部份的生物鹼。


生物鹼的分類

与大多数其他天然化合物相比,生物碱的特征在于其丰富的结构多样性,没有统一分类。

類別 主要結構 主要合成路線 例子
與含氮雜環生物鹼(真正生物鹼)
吡咯烷 類衍生物
Pyrrolidine structure.svg
鳥氨酸精氨酸腐胺 → N-甲基腐胺 → N-methyl-Δ1-pyrroline Cuscohygrine, hygrine, hygroline, stachydrine
托烷 類衍生物
Tropane numbered.svg
阿托品
原子取代於位置 3, 6 或 7
鳥氨酸或精氨酸→腐胺→N-甲基腐胺→N-甲基-Δ1-吡咯烷酮 Atropine, scopolamine, hyoscyamine
可卡因
原子取代於位置 2, 3
Cocaine, ecgonine
吡咯里西啶 類衍生物
Pyrrolizidine.svg
鳥氨酸,精氨酸→腐→類精脒→惹卓裂鹼 Retronecine, heliotridine, laburnine
一元羧酸的複合酯 Indicine, lindelophin, sarracine
大環內二酯 Platyphylline, trichodesmine
1-氨基吡咯烷類 (lolines) L-脯氨酸+ L-高絲氨酸→N-(3-氨基-3-羧丙基)脯氨酸→降黑麥草堿 Loline, N-formylloline, N-acetylloline
哌啶 類衍生物
Piperidin.svg
賴氨酸屍胺 → Δ1-piperideine Sedamine, lobeline, anaferine, piperine
辛酸 → coniceine → 毒芹碱 Coniine, coniceine
類衍生物
Quinolizidine.svg
羽扇豆寧 賴氨酸屍胺 → Δ1-piperideine Lupinine, nupharidin
金雀花鹼 Cytisine
鷹爪豆鹼 Sparteine, lupanine, anahygrine
苦參鹼 Matrine, oxymatrine, allomatridine
苦豆鹼 Ormosanine, piptantine
吲哚聯啶 類衍生物
Indolizidine.svg
賴氨酸 → δ-semialdehyde of Α-氨基己二酸pipecolic acid → 1 indolizidinone Swainsonine, castanospermine
吡啶 類衍生物
Pyridine.svg
吡啶簡單衍生物 烟酸 → dihydronicotinic acid → 1,2-dihydropyridine Trigonelline, ricinine, arecoline
多環芳烴冷凝吡啶衍生物 Nicotine, nornicotine, anabasine, anatabine
多環芳烴冷凝吡啶衍生物 Actinidine, gentianine, pediculinine
Sesquiterpene pyridine derivatives 烟酸, 異亮氨酸 Evonine, hippocrateine, triptonine
異喹啉 類衍生物及相關生物鹼
Isoquinoline numbered.svg
Simple derivatives of isoquinoline Tyrosine or 苯丙氨酸多巴胺 or 酪胺 (for alkaloids Amarillis) Salsoline, lophocerine
Derivatives of 1- and 3-isoquinolines N-methylcoridaldine, noroxyhydrastinine
Derivatives of 1- and 4-phenyltetrahydroisoquinolines Cryptostilin
Derivatives of 5-naftil-isoquinoline Ancistrocladine
Derivatives of 1- and 2-benzyl-izoquinolines Papaverine, laudanosine, sendaverine
Cularine group Cularine, yagonine
Pavines and isopavines Argemonine, amurensine
Benzopyrrocolines Cryptaustoline
Protoberberines Berberine, canadine, ophiocarpine, mecambridine, corydaline
Phthalidisoquinolines Hydrastine, narcotine (Noscapine)
Spirobenzylisoquinolines Fumaricine
Ipecacuanha alkaloids Emetine, protoemetine, ipecoside
Benzophenanthridines Sanguinarine, oxynitidine, corynoloxine
Aporphines Glaucine, coridine, liriodenine
Proaporphines Pronuciferine, glaziovine
Homoaporphines Kreysiginine, multifloramine
Homoproaporphines Bulbocodine
嗎啡s 嗎啡, 可待因, 蒂巴因, 青藤碱
Homomorphines Kreysiginine, androcymbine
Tropoloisoquinolines Imerubrine
Azofluoranthenes Rufescine, imeluteine
Amaryllis alkaloids Lycorine, ambelline, tazettine, galantamine, montanine
Erythrina alkaloids Erysodine, erythroidine
Phenanthrene derivatives Atherosperminine
Protopines Protopine, oxomuramine, corycavidine
Aristolactam Doriflavin
噁唑 類衍生物[
Oxazole structure.svg
Tyrosinetyramine Annuloline, halfordinol, texaline, texamine
異噁唑 類衍生物
Isoxazole structure.png
Ibotenic acidMuscimol Ibotenic acid, Muscimol
噻唑 類衍生物
Thiazole structure.svg
1-Deoxy-D-xylulose 5-phosphate (DOXP), tyrosine, cysteine Nostocyclamide, thiostreptone
喹唑啉 類衍生物
Quinazoline numbered.svg
3,4-Dihydro-4-quinazolone derivatives Anthranilic acid or phenylalanine or ornithine Febrifugine
1,4-Dihydro-4-quinazolone derivatives Glycorine, arborine, glycosminine
Pyrrolidine and piperidine quinazoline derivatives Vazicine (peganine)
吖啶 類衍生物
Acridine.svg
Anthranilic acid Rutacridone, acronicine
喹啉 類衍生物
Quinoline numbered.svg
Simple derivatives of quinoline derivatives of 2 – quinolones and 4-quinolone Anthranilic acid → 3-carboxyquinoline Cusparine, echinopsine, evocarpine
Tricyclic terpenoids Flindersine
Furanoquinoline derivatives Dictamnine, fagarine, skimmianine
Quinines Tryptophantryptaminestrictosidine (with secologanin) → korinanteal → cinhoninon Quinine, quinidine, cinchonine, cinhonidine
吲哚 類衍生物
Indole numbered.svg
異戊二烯吲哚生物鹼
Simple indole derivatives Tryptophantryptamine or 5-hydroxitriptofan Serotonin, psilocybin, dimethyltryptamine (DMT), bufotenin
Simple derivatives of β-carboline Harman, harmine, harmaline, eleagnine
Pyrroloindole alkaloids Physostigmine (eserine), etheramine, physovenine, eptastigmine
萜類吲哚生物鹼'
Ergot alkaloids Tryptophan → chanoclavine → agroclavine → elimoclavine → paspalic acidlysergic acid Ergotamine, ergobasine, ergosine
單萜吲哚生物鹼
Corynanthe type alkaloids Tryptophantryptaminestrictosidine (with secologanin) Ajmalicine, sarpagine, vobasine, ajmaline, yohimbine, reserpine, mitragynine, group strychnine and (Strychnine brucine, aquamicine, vomicine )
Iboga-type alkaloids Ibogamine, ibogaine, voacangine
Aspidosperma-type alkaloids Vincamine, vinca alkaloids, vincotine, aspidospermine
咪唑 類衍生物
Imidazole structure.svg
Directly from histidine Histamine, pilocarpine, pilosine, stevensine
嘌呤 類衍生物
9H-Purine.svg
Xanthosine (formed in purine biosynthesis) → 7 methylxantosine → 7-methyl xanthinetheobrominecaffeine Caffeine, theobromine, theophylline, saxitoxin
側鏈上含氮原子的生物側鏈鹼
β-苯乙胺 類衍生物
Phenylethylamine numbered.svg
Tyrosine or phenylalaninedioxyphenilalaninedopamineadrenaline and mescaline tyrosinetyramine phenylalanine → 1-phenylpropane-1,2-dione → cathinoneephedrine and pseudoephedrine Tyramine, ephedrine, pseudoephedrine, mescaline, cathinone, catecholamines (adrenaline, noradrenaline, dopamine)
秋水仙素 類衍生物
Colchicine.svg
Tyrosine or phenylalaninedopamineautumnalinecolchicine Colchicine, colchamine
毒蕈鹼
Muscarine.svg
Glutamic acid → 3-ketoglutamic acid → muscarine (with pyruvic acid) Muscarine, allomuscarine, epimuscarine, epiallomuscarine
芐胺
Benzylamine.svg
Phenylalanine with valine, leucine or isoleucine Capsaicin, dihydrocapsaicin, nordihydrocapsaicin, vanillylamine
多胺生物鹼
腐胺 衍生物
Putrescine.svg
ornithineputrescinespermidinespermine Paucine
亞精胺 衍生物
Spermidine.svg
Lunarine, codonocarpine
精胺 衍生物
Spermine.svg
Verbascenine, aphelandrine
Peptide (cyclopeptide) alkaloids
Peptide alkaloids with a 13-membered cycle Nummularine C type From different amino acids Nummularine C, Nummularine S
Ziziphine type Ziziphine A, sativanine H
Peptide alkaloids with a 14-membered cycle Frangulanine type Frangulanine, scutianine J
Scutianine A type Scutianine A
Integerrine type Integerrine, discarine D
Amphibine F type Amphibine F, spinanine A
Amfibine B type Amphibine B, lotusine C
Peptide alkaloids with a 15-membered cycle Mucronine A type Mucronine A
Pseudoalkaloids (terpenes and steroids)
Diterpenes
Isoprene.svg
Lycoctonine type Mevalonic acidizopentenilpyrophosfategeranyl pyrophosphate Aconitine, delphinine
Steroids
Cyclopentenophenanthrene.svg
Cholesterol, arginine Solasodine, solanidine, veralkamine, batrachotoxin

引用

来源

  • Aniszewski, Tadeusz. Alkaloids – secrets of life. Amsterdam: Elsevier. 2007. ISBN 978-0-444-52736-3. 
  • Begley, Tadhg P. Encyclopedia of Chemical Biology. Wiley. 2009. ISBN 978-0-471-75477-0. doi:10.1002/cbic.200900262. 
  • Brossi, Arnold. The Alkaloids: Chemistry and Pharmacology. Academic Press. 1989. 
  • Dewick, Paul M. Medicinal Natural Products. A Biosynthetic Approach 2nd. Wiley. 2002. ISBN 0-471-49640-5. 
  • Fattorusso, E.; Taglialatela-Scafati, O. Modern Alkaloids: Structure, Isolation, Synthesis and Biology. Wiley-VCH. 2008. ISBN 978-3-527-31521-5. 
  • Grinkevich, N. I.; Safronich, L. N. The chemical analysis of medicinal plants: Proc. allowance for pharmaceutical universities. M. 1983. 
  • Hesse, Manfred. Alkaloids: Nature's Curse or Blessing?. Wiley-VCH. 2002. ISBN 978-3-906390-24-6. 
  • Knunyants, I. L. Chemical Encyclopedia. Soviet Encyclopedia. 1988 [2014-08-23]. (原始内容存档于2021-03-07). 
  • Orekhov, A. P. Chemistry alkaloids Acad. 2. M.: USSR. 1955. 
  • Plemenkov, V. V. Introduction to the Chemistry of Natural Compounds. Kazan. 2001. 
  • Saxton, J. E. The Alkaloids. A Specialist Periodical Report. London: The Chemical Society. 1971. 
  • Veselovskaya, N. B.; Kovalenko, A. E. Drugs. Moscow: Triada-X. 2000. 
  • Wink, M. Mode of action and toxicology of plant toxins and poisonous plants. Mitt. Julius Kühn-Inst. 2009, 421: 93–112 [18 March 2014]. (原始内容存档于2014-03-18). 

外部連結

参见


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